X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: Evidence from segregation analysis for dependence on X chromosome inactivation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 88, Issue 18, 1991, Pages 8198-8202

  Bu, Xiangdong ^a   Rotter, Jerome I ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

Cytoplasmic inheritance; Reduced penetrance; Two locus inheritance

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; EXTRACHROMOSOMAL INHERITANCE; FEMALE; HEREDITARY OPTIC ATROPHY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKED DISORDER;

DNA, MITOCHONDRIAL; DOSAGE COMPENSATION (GENETICS); FEMALE; GENE EXPRESSION; HETEROZYGOTE; HUMAN; LINKAGE (GENETICS); MALE; OPTIC ATROPHIES, HEREDITARY; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; X CHROMOSOME;

EID: 0025820109     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.88.18.8198     Document Type: Article

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